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[家族性腺瘤性息肉病轻度形式中的弥漫性胃癌。相关性还是巧合?]

[Diffuse stomach cancer in the minor form of familial adenomatosis coli. Correlation or coincidence?].

作者信息

Polensky A, Nekarda H, Riecken E O

机构信息

Medizinische Klinik, Klinikum Steglitz der Freien Universität Berlin.

出版信息

Z Gastroenterol. 1988 Dec;26(12):737-43.

PMID:3245252
Abstract

We report about a 66-year-old female patient with Gardner syndrome, a special form of familial adenomatosis coli, and a stomach carcinoma occurring at the same time. Recently, there have been more reports about duodenal carcinomas and stomach polyps in intestinal adenomatosis due to an improvement in diagnostic methods. The concomitant occurrence of a stomach carcinoma is, however, a very rare finding. So far, altogether 10 case histories have been published world-wide. The case presented here and a review of the literature again lend current interest to the hypothesis formulated by Amman in 1976 according to which the occurrence of a stomach carcinoma in connection with a Gardner syndrome/familial adenomatosis coli, particular in the minor form of this entity (recessive hereditary course, less than 100 polyps in the intestines, occurrence of polyps in old age) must be regarded as an additional characteristic of this disease. On the basis of this hypothesis, all adenomatosis patients should undergo gastroscopy.

摘要

我们报告了一例66岁女性患者,其同时患有加德纳综合征(一种家族性腺瘤性息肉病的特殊形式)和胃癌。近年来,由于诊断方法的改进,关于肠腺瘤病中十二指肠癌和胃息肉的报道增多。然而,胃癌与之同时发生的情况非常罕见。迄今为止,全球共发表了10例相关病例报告。本文所呈现的病例以及文献综述再次引发了人们对阿曼于1976年提出的假说的关注,该假说认为,与加德纳综合征/家族性腺瘤性息肉病相关的胃癌,尤其是该疾病的轻症形式(隐性遗传病程、肠道息肉少于100个、息肉在老年时出现),应被视为该疾病的一个额外特征。基于这一假说,所有腺瘤病患者都应接受胃镜检查。

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